Results 61 to 70 of about 4,881 (207)

The contribution of maternal serum markers in the early prenatal diagnosis of molar pregnancies [PDF]

open access: yes, 2017
The aim of this study was to evaluate the usefulness of maternal serum markers in the early prenatal diagnosis of molar pregnancies. The ultrasound features, cytogenetic and histopathological findings of 10 cases of molar pregnancy diagnosed at 11-13 ...
Bersinger, N.A.   +3 more
core  

The impact of metabolic risk management on recurrence of urinary stones [PDF]

open access: yes, 2012
Introduction: Urinary stone disease is a common urologic problem and recurrence in stone formation is a very familiar issue to urologists. Although recurrence in stone formation has been linked to metabolic abnormalities, it can be accessible by ...
Akin, Yigit   +4 more
core   +3 more sources

Downregulation of Chromosome 19 miRNA Cluster and the Tumor‐Suppressive Role of miR‐517a‐3p in Choriocarcinoma

open access: yesCancer Science, Volume 116, Issue 12, Page 3473-3486, December 2025.
Chromosome 19 microRNA cluster was downregulated in choriocarcinoma compared with complete hydatidiform mole. miR‐517a‐3p reduced the proliferation, migration, and invasion abilities of choriocarcinoma cell lines. Downregulation of SRSF1, targeted by miR‐517a‐3p, suppressed the malignant potential of choriocarcinoma cell lines. ABSTRACT Choriocarcinoma
Yuki Nishiko   +14 more
wiley   +1 more source

Molecular cytogenetic analysis of a hydatidiform mole with coexistent fetus: a case report

open access: yesJournal of Medical Case Reports, 2019
Background A hydatidiform mole with a coexisting fetus is a rare condition that commonly occurs as either a partial mole with fetus or a twin pregnancy comprising a complete mole and normal fetus.
Nozomi Uemura   +8 more
doaj   +1 more source

Clinical and histological observations of chorioepithelioma and hydatidiform mole [PDF]

open access: yes, 1961
1. Clinical and histological evaluation of so-called chorioepithelioma malignum and hydatidiform mole has been made on the cases treated at the Department of Obstetrics and Gynecology, Okayama University Hospital during the 20year period friom 1939 to ...
Hashimoto, Kiyoshi   +3 more
core   +1 more source

Six New Cases of 22q13.2 Gain Including TFC20: First Report of Triplication and Smallest Duplication Associated With Neurodevelopmental Delays

open access: yesClinical Genetics, Volume 108, Issue 6, Page 731-741, December 2025.
This study reports six new cases of 22q13.2 duplication and triplication, including the TCF20 gene, associated with neurodevelopmental disorders and various morphological and systemic abnormalities. The findings suggest a variable expressivity, but their complete penetrance remains uncertain compared to well‐established loss‐of‐function variants ...
Etienne Bizot   +13 more
wiley   +1 more source

Precision Diagnosis and Individualized Therapy of Non‐Gestational Choriocarcinoma Invading the Corpus Uteri and Cervix: A Case Report and Literature Review

open access: yesCancer Reports, Volume 8, Issue 11, November 2025.
ABSTRACT Background Non‐gestational choriocarcinoma (NGCC) is a rare type of malignant tumor. Primary lesions are typically detected in the ovary and rarely invade the corpus uteri and cervix. NGCC usually has a poor prognosis due to the difficulty in achieving early and accurate diagnoses because of its rarity.
Jiahui Ma   +5 more
wiley   +1 more source

Expression of Pro-Apoptotic Bax and Anti-Apoptotic Bcl-2 Proteins in Hydatidiform Moles and Placentas With Hydropic Changes

open access: yesActa Medica Iranica, 2019
Morphologic examination still forms the main diagnostic tool in the differential diagnosis of molar placentas. However the criteria are subjective and show considerable inter-observer variability among pathologists.
Alireza Khooei   +5 more
doaj  

Single haplotype assembly of the human genome from a hydatidiform mole [PDF]

open access: yes, 2014
A complete reference assembly is essential for accurately interpreting individual genomes and associating variation with phenotypes. While the current human reference genome sequence is of very high quality, gaps and misassemblies remain due to ...
Agarwala, Richa   +12 more
core   +2 more sources

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